HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane → HCID 86590399, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1S,4S)-2-Boc-2,5-diazabicyclo[2.2.1]heptane | HCID 11521263 | — |
| Reactant | Methyl 3,6-dichloropyridazine-4-carboxylate | HCID 17861811 | — |
| Product | HCID 86590399 | HCID 86590399 | 41% |
Reaction Steps
Methyl 3,6-dichloropyridazine-4-carboxylate and tert-butyl (1S,4S)-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate, prepared as described in (J. Med. Chem., (1988) 31, 1598-1611), were processed as described in Example 2A to provide the title compound (41% yield). 1H NMR (CDCl3, 300 MHz) δ 1.42 (s, 4.5H), 1.47 (s, 4.5H), 1.90-2.11 (m, 2H), 2.86 (d, J=9.93 Hz, 1H), 3.40-3.62 (m, 2H), 3.72 (d, J=9.90 Hz, 1H), 3.93 (s, 3H), 3.51 (s, 0.5H), 4.63 (s, 0.5H), 5.05-5.15 (m, 1H), 7.49 (s, 1H); MS (DCI/NH3) m/z 368 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07265115B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-fe78703507964e839b84e331240f0a45 |
| Source note | uspto-grants-2007_09 |